Demonstration of both beta 1- and beta 2-adrenoceptors mediating negative chronotropic effects on spontaneous activity in isolated bovine mesenteric lymphatics

Microvasc Res. 1990 Jan;39(1):50-9. doi: 10.1016/0026-2862(90)90058-y.

Abstract

The pharmacological classification of beta-adrenoceptor subtypes in isolated bovine mesenteric lymphatics was studied by using various beta-adrenoceptor agonists and antagonists. Isoproterenol (ISP) (10(-10)-10(-8) M) produced dose-dependent negative chronotropic effects on the rhythm of spontaneous contractions in the lymphatic preparation. The ISP-induced effects were dose-dependently blocked by pretreatment with 10(-8)-10(-7) M metoprolol (a selective beta 1 antagonist) as well as 10(-8)-10(-7) M propranolol (a beta 1 and beta 2 antagonist). Dobutamine (a selective beta 1 agonist) caused a dose-dependent negative chronotropic effect, which was significantly blocked by pretreatment with 10(-8) M metoprolol. Salbutamol and procaterol (selective beta 2 agonists) also produced dose-dependent negative chronotropic effects, which were dose-dependently inhibited by pretreatment with 10(-8)-10(-7) M propranolol, but not by 10(-7) M metoprolol. The decreasing order of the relative potency was as follows: ISP greater than procaterol greater than salbutamol greater than dobutamine. These results suggest that bovine mesenteric lymphatics contain both beta 1- and beta 2-adrenoceptors and that both subtypes can produce a negative chronotropic effect on the rhythm of spontaneous contractions, when stimulated.

MeSH terms

  • Adrenergic beta-Agonists / pharmacology
  • Adrenergic beta-Antagonists / pharmacology
  • Animals
  • Cattle
  • Depression, Chemical
  • In Vitro Techniques
  • Lymphatic System / drug effects
  • Lymphatic System / physiology*
  • Mesentery
  • Muscle Contraction / drug effects
  • Muscle Contraction / physiology
  • Receptors, Adrenergic, beta / classification
  • Receptors, Adrenergic, beta / drug effects
  • Receptors, Adrenergic, beta / physiology*

Substances

  • Adrenergic beta-Agonists
  • Adrenergic beta-Antagonists
  • Receptors, Adrenergic, beta